GRD BIOMECHANICS

FDA Device Registration & Listing · Deland, FL, US · Registration 3014826829

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014826829
FEI Number
3014826829
Entity Name
GRD BIOMECHANICS
City/State/Country
Deland, FL, US
Establishment Address
101 N. Woodland Blvd, STE A301, Deland, FL 32720, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
GRD Biomechanics (Owner Number: 10058585)
Owner / Operator Contact Address
101 N Woodland Blvd, STE A301, Deland, FL 32720, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ascend with VRS Ascend

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2018-10-22

Official Correspondent

Michael Geldart

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GRD Biomechanics
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014826829. Last updated year: 2026. Please use registration number 3014826829 when referencing this establishment in official correspondence.
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